Dietary L-carnitine suppresses mitochondrial branched-chain keto acid dehydrogenase activity and enhances protein accretion and carcass characteristics of swine

• Published in: Journal of animal science 2001-12, Vol.79 (12), p.3104-3112
• Main Authors: Owen, K. Q, Jit, H, Maxwell, C. V, Nelssen, J. L, Goodband, R. D, Tokach, M. D, Tremblay, G. C, Koo, S. I
• Format: Article
• Language: English
• Subjects: 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide); Adipose Tissue - anatomy & histology; Adipose Tissue - drug effects; Amino acids; Amino Acids, Branched-Chain - metabolism; Animal productions; Animals; Biological and medical sciences; Body Composition - drug effects; Carnitine - administration & dosage; Carnitine - pharmacology; Dietary supplements; Female; Fundamental and applied biological sciences. Psychology; Hepatocytes - metabolism; Hogs; Ketone Oxidoreductases - antagonists & inhibitors; Ketone Oxidoreductases - metabolism; Mitochondria, Liver - enzymology; Mitochondria, Muscle - enzymology; Multienzyme Complexes - antagonists & inhibitors; Multienzyme Complexes - metabolism; Muscle, Skeletal - drug effects; Muscle, Skeletal - growth & development; Palmitates - metabolism; Pork; Protein Biosynthesis; Proteins; Pyruvate Carboxylase - metabolism; Swine - growth & development; Swine - metabolism; Terrestrial animal productions; Vertebrates
• ISSN: 0021-8812; 1525-3163; 0021-8812
• DOI: 10.2527/2001.79123104x

A trial was conducted to biochemically explain the decreased lipid deposition and increased protein accretion observed in pigs fed carnitine. Our hypothesis was that an increase in the ratio of acetyl CoA:CoA-SH produced by stimulation of fatty acid oxidation by supplemental L-carnitine may decrease branched-chain alpha-keto acid dehydrogenase activity and increase pyruvate carboxylase activity. Such changes could reduce oxidative loss of branched-chain amino acids and provide more carbons for amino acid biosynthesis. Yorkshire gilts (n = 36; 12 per treatment) were fed a control diet or diets containing either 50 or 125 ppm of added L-carnitine during growth from 56 to 120 kg. After slaughter, the semitendinosus muscle and liver were collected for isolation of mitochondria and hepatocytes. Increasing dietary L-carnitine did not influence growth performance (P > 0.10) but linearly decreased (P < 0.05) 10th rib backfat thickness and increased (linear, P < 0.05) percentages of lean and muscle. The rates of [1-(14)G]palmitate oxidation in isolated hepatocytes and isolated mitochondria, and incorporation of [35S]methionine into the acid insoluble fraction of isolated hepatocytes were increased (linear, P < 0.01) in pigs fed L-carnitine. Flux through branched-chain alpha-keto acid dehydrogenase linearly decreased (P < 0.01) in isolated liver and muscle mitochondria with increasing dietary carnitine. Flux through pyruvate carboxylase was increased (linear, P < 0.01) in isolated mitochondria from liver of pigs fed carnitine, and assays with particle-free extracts indicated that the amount of mitochondrial pyruvate carboxylase was tripled by feeding carnitine (linear, P < 0.01). The association of increased protein accretion and reduced backfat thickness with greater rates of palmitate oxidation, more rapid flux through pyruvate carboxylase, and reduced flux through branched-chain alpha-keto acid dehydrogenase suggests pigs fed carnitine are more able to use fat for energy, divert carbon toward synthesis of amino acids, and spare branched-chain amino acids for protein synthesis.